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ESTRO 35 2016 S157

______________________________________________________________________________________________________

survivors generally have an increased risk of new tumor

formation.

Proffered Papers: Clinical 8: Adult and paediatric CNS

malignancies

OC-0345

Patterns of failure after radiotherapy in pediatric

ependymoma: correlation with dose parameters

F. Tensaouti

1

UMR 825 Inserm / Université Toulouse Iii - Paul Sabatier,

Research, Toulouse, France

1

, A. Ducassou

2

, S. Bolle

3

, X. Muracciole

4

, B.

Coche-dequeant

5

, L. Claude

6

, S. Supiot

7

, C. Alapetite

8

, V.

Bernier

9

, A. Huchet

10

, C. Kerr

11

, E. Le Prise

12

, G. Truc

13

, E.

Regnier

14

, S. Chapet

15

, A. Lisbona

7

, G. Hangard

2

, A. Laprie

2

2

Institut Claudius Regaud Toulouse- Iuct Oncopole,

Radiotherapy, Toulouse, France

3

Institut Gustave Roussy- Villejuif, Radiotherapy, Paris,

France

4

CHU La Timone, Radiotherapy, Marseille, France

5

Centre Oscar Lambret, Radiotherapy, Lille, France

6

Centre Léon Bérard, Radiotherapy, Lyon, France

7

Institut De Cancérologie De L’ouest, Radiotherapy, Nantes,

France

8

Institut Curie, Radiotherapy, Paris, France

9

Institut De Cancérologie De Lorraine- Alexis Vautrin,

Radiotherapy, Nancy, France

10

CHU Bordeaux, Radiotherapy, Bordeaux, France

11

Institut Du Cancer De Montpellier, Radiotherapy,

Montpellier, France

12

Centre Eugène Marquis, Radiotherapy, Rennes, France

13

Centre Georges François Leclerc, Radiotherapy, Dijon,

France

14

Institut Jean Godinot, Radiotherapy, Reims, France

15

CHU Tours, Radiotherapy, Tours, France

Purpose or Objective:

The aim of this study was to

investigate the patterns of failure after radiotherapy for

pediatric intracranial ependymoma and their correlation to

dose parameters.

Material and Methods:

Between 2000 and 2013, 206 patients

with intracranial ependymoma were treated in the 13 french

reference pediatric radiotherapy centers . The magnetic

resonance imaging obtained at recurrence were registered

with the original planning CT for topographic analysis of the

patterns failure. Clinical target volume (CTV) and planning

target volume (PTV) margins were extracted ; several

dosimetric quality indices were derived from Dose Volume

Histogram (DVH) to compare relapse with no-relapse patient.

Results:

With a median follow-up of 44.81 months (95% CI

[36.80; 56.51]), 85 (41.3%) patients presented with

recurrence. The topographic analysis of patterns of failure

showed 50 (58.8%) patients with local recurrence in the

radiation field (LF), 6 (4.1%) in the edge of field (EFG), 6

(7.1%) were loco-regional outside the field (LRF), 8 (9.4%) in

spine (SF), 5 supratentorial (SUF) and 10 (11.8%) local and

distant (LDF). The median prescription dose was respectively:

55.8 Gy [50.4; 60] in LF, 54 Gy [48.6; 59.4] in EF, 56.7 Gy

[50.4; 60] in LRF, 54 Gy [50.4; 59.4] in LDF, 59.4 Gy [48.6-

59.4] in SUF and 56.7Gy [54; 60] in SF. The median PTV

margins was 0.5 mm [0.3; 1]. The median Coverage index and

The Target Coverage index of the PTV were both lower in the

relapse group as they were respectively 0.97 and 94.8% in the

relapse group compared with 0.98 and 95.99% in the no-

relapse group. The median Homogeneity index was 0.097 in

the relapse group versus 0.091 in the no-relapse group. The

median volume of relapse was 1.29 cc [0.11; 27] in the LF

group, with a median dose of 58.81 Gy [50.86; 61.38].

Conclusion:

In patients with intracranial ependymoma, local

failure in the tumor bed was the major pattern of failure.

The preliminary results showed that all dosimetric indices on

the PTV were worse in the relapse group. Improving the

coverage of target volume may be an effective way to reduce

the local failures. Thus a complementary correlation of

relapse patterns with dose parameters to PTV and organs at

risks and the irradiation techniques is under statistical

analysis and final results will be presented at the meeting.

OC-0346

Pediatric diffuse intrinsic pontine glioma re-irradiation:

better survival and better time

L. Gandola

1

Fondazione IRCCS Istituto Nazionale dei Tumori, Radiation

Oncology- Pediatric Radiotherapy Unit, Milan, Italy

1

, E. Pecori

1

, V. Biassoni

2

, B. Diletto

1

, E.

Schiavello

2

, S. Meroni

3

, F. Spreafico

2

, E. Pignoli

3

, M.

Massimino

2

2

Fondazione IRCCS Istituto Nazionale dei Tumori, Pediatric

Oncology, Milan, Italy

3

Fondazione IRCCS Istituto Nazionale dei Tumori, Medical

Physics, Milan, Italy

Purpose or Objective:

Since 2009 we launched a strategy for

children with centrally reviewed MRI diagnosis of diffuse

intrinsic pontine glioma (DIPG) implying the intravenous

administration of vinorelbine with nimotuzumab –an anti-

EGFR monoclonal antibody- weekly, for a total of 12 weeks,

during radiotherapy delivery of 54 Gy, 1.8 Gy/fraction daily.

After radiotherapy completion, vinorelbine and nimotuzumab

were administered any other week until tumor progression or

for a total of two years. In the attempt to improve survival

and quality of life of our children, a protocol amendment in

July 2011 introduced re-irradiation at relapse/progression.

Material and Methods:

Local re-irradiation consisted of 19.8

Gy, fractionated over 11 days. A 3DCRT with 5-6 coplanar

beams was adopted with a beam geometry possibly not

overlapping that of the first line irradiation; the most

demanding planning issue of re-irradiation was to meet optic

chiasm dose constraints. Three additional children were re-

irradiated to distant sites of relapse, spine (2) or ventricular

system at doses of 36 Gy or 54 Gy respectively.

Results:

Of the 39 patients treated from 8/2009, 28 had local

(23) or disseminated (5) progression and 18 were given local

(15) or distant (3) relapse re-irradiation at a median of 8

months after first radiotherapy (2.5-19 months). Reasons for

not re-irradiating the other 10 children were: progression

before July 2011 (4), parents refusal (4), too poor Lansky

status (2); median PFS and progression site were not

different in the two subgroups. Survival after re-irradiation

lasted between two weeks and 14 months, median 6 months,

and determined a statistically difference in median OS

between the two groups of re-irradiated or not children,

being 16 and 12 months, respectively (P=0.004). In 16

radiologically evaluated patients, re-irradiation induced:

reduction of tumor volume in 8, stable volume in 3 while 5

had progression; 13 had symptom amelioration and 12 steroid

suspension. Volume reductions were obtained in 7/8 children

that have shown the same response after first line irradiation

while one was obtained after stable disease in first line

treatment. No adverse event was reported and all children

were re-irradiated as outpatients .

Conclusion:

Re-irradiation after relapse/progression

represented a significant benefit for both OS and quality of

life of children with DIPG with symptom amelioration in

13/18. This option is worth to be offered also in case of

disseminated progression.

Partially supported by Associazione Italiana per la Ricerca sul

Cancro (AIRC)

OC-0347

Outcome and prognosticators in adult patients with

medulloblastoma: a Rare Cancer Network study

B. Atalar

11

Acıbadem University, Department of Radiation Oncology,

Istanbul, Turkey

1

, M. Ozsahin

2

, J. Call

3

, A. Napieralska

4

, S. Kamer

5

,

V. Salvador

6

, P. Erpolat

7

, L. Negretti

2

, Y.L. Ramstad

8

, C.

Onal

9

, S. Akyurek

10

, G. Ugurluer

1

, B. Baumert

11,12

, S. Servagi-

Vernat

13

, R.C. Miller

14

, E. Ozyar

1

, T. Sio

15

2

Centre Hospitalier Universitaire Vaudois, Department of

Radiation Oncology, Lausanne, Switzerland